Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,440 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,440 in last 12 months

Showing 1694116960 of 46,762 recalls

DrugJuly 31, 2020· The Mentholatum Company

Recalled Item: Red Cross Oral Pain (Oral Anesthetic benzocaine 20%) Recalled by The...

The Issue: Labeling; Not Elsewhere Classified: The Mentholatum Company is initiating a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 31, 2020· MicroPort Orthopedics Inc.

Recalled Item: PROFEMUR Titanium and Cobalt Chrome modular necks Recalled by MicroPort...

The Issue: MicroPort Orthopedics Inc. is voluntarily recalling any existing inventory...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2020· Klarity Medical Products LLC

Recalled Item: Klarity Vacuum Bags Recalled by Klarity Medical Products LLC Due to Vacuum...

The Issue: Vacuum bags potentially may not hold their vacuum adequately for needed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 30, 2020· Albek De Mexico S.A. De C.V.

Recalled Item: Assured Instant Hand Sanitizer Aloe & Moisturizers (Ethyl Alcohol 70%...

The Issue: CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2020· Albek De Mexico S.A. De C.V.

Recalled Item: Modesa INSTANT HAND SANITIZER with Moisturizers and Aloe Vera (ethyl...

The Issue: CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2020· Albek De Mexico S.A. De C.V.

Recalled Item: NuuxSan Instant ANTIBACTERIAL HAND SANITIZER Recalled by Albek De Mexico...

The Issue: CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2020· Albek De Mexico S.A. De C.V.

Recalled Item: NEXT ADVANCED ANTIBACTERIAL HAND SANITIZER (Ethyl Alcohol 70%) Recalled by...

The Issue: CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2020· Albek De Mexico S.A. De C.V.

Recalled Item: Assured Instant Hand Sanitizer Vitamin E and Aloe (Ethyl Alcohol 70% v/v)...

The Issue: CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2020· Ecolab Inc

Recalled Item: Hand Sanitizer (Alcohol 80% v/v) topical solution Recalled by Ecolab Inc Due...

The Issue: Discoloration and Presence of Foreign Substance

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 30, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgM Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: Device did not meet the updated EUA packet requirements for positive percent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· Cardinal Health 200, LLC

Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...

The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 10 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 2 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund